Homework Answers
Here is the solution of your question. If you have any doubt or need any clarification please comment in comment box and will definitely resolve your query. If you find useful please upvote it. Thanks in advance.
Add Answer to:
(V) ! show the preparation of the following compounds
(v) 2-heptanone starting from acetylene (vi) Cis-3-hexene...
Show the reagents to convert acetylene to cis -3-hexene
Show the reagents to convert acetylene to cis -3-hexene
Name the product of the following reaction. cis-3-Hexene. trans-3-Hexene. 1-Hexene. trans-2-Hexene. cis-2-Hexene. Addition of 2 mol...
Name the product of the following reaction. cis-3-Hexene. trans-3-Hexene. 1-Hexene. trans-2-Hexene. cis-2-Hexene. Addition of 2 mol of HCl to 1-butyne would yield: CH_3CH_2CH_2CHCl_2 CH_3CH_2CCI_2CH_3 CH_3CH_2CHCICH_2Cl CH_3CH_2CH=CHCI CH_3CHCICHCICH_3 In the presence of excess hydrogen bromide, what is the major product of the addition of HBr to acetylene? 1, 3-dibromoethane 1-bromoethane 1, 1-dibromoethane 1, 2-dibromoethane 2-bromoethane Which of the following compounds is the major product when 1-hexyne is treated with excess HBr? 1, 1-dibromohexane 1, 1-dibromohexene 1, 2-dibromohexene 1, 2-dibromohexane 2, 2-dibromohexane
2. Which of the following compounds exhibit cis/trans Isomer CIS and transforms of the compounds that...
2. Which of the following compounds exhibit cis/trans Isomer CIS and transforms of the compounds that do exhibit Isomers s exhibit cis/trans isomerism? Explain why. Draw the a) Methylcyclobutane b) 3-ethyl-3-hexene c) 1-ethyl-3-methylcyclopentane d) 2,3-dimethylpentane e) 2,3-dichloro-2-hexene f) 2-butyne
10-2 Using acetylene as the starting material, show how you would synthesize the following compounds а)...
10-2 Using acetylene as the starting material, show how you would synthesize the following compounds а) b) but-2-yne с) d)
_________________________________________________________________________________________________________________________________ d. Prepare octane from 1-pentyne, indicate each needed reagents. e. Synthesize cis-2-hexene from 1-pentyne and...
_________________________________________________________________________________________________________________________________
d. Prepare octane from 1-pentyne, indicate each needed
reagents.
e. Synthesize cis-2-hexene from 1-pentyne and an alkyl
halide.
f. Synthesize trans-2-hexene from 1-pentyne and an alkyl
halide.
Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
VI. Starting from acetylene (CH C H) and using any needed reagents to synthesize the following...
VI. Starting from acetylene (CH C H) and using any needed reagents to synthesize the following molecule: Show every single step of the synthesis (10 pts)
Sintetize 1) hexene from ethyne 2) Cis-3-hexene from ch2-ch2-Br
Sintetize 1) hexene from ethyne 2) Cis-3-hexene from ch2-ch2-Br
please explain Problem 5 (10 pts) Starting from acetylene propose a synthesis of both cis-3-heptene and...
please explain
Problem 5 (10 pts) Starting from acetylene propose a synthesis of both cis-3-heptene and trans-3-heptene.
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis...
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
Propose synthetic pathways for the laboratory preparation of the following compounds from the specified substrates. Show...
Propose synthetic pathways for the laboratory preparation of the
following compounds from the specified substrates. Show all steps
complete with reagents and structures of products. Use any required
aliphatic and inorganic reagents.
i) propanal from 3-hexene j) 2-pentanone from butanoic acid k) 3-ethyl-3-pentanol from ethyl propanoate 1) 7-(N,N-dimethylamino)-2-heptanol from 1-methylcyclohexene
Name the product of the following reaction. cis-3-Hexene. trans-3-Hexene. 1-Hexene. trans-2-Hexene. cis-2-Hexene. Addition of 2 mol of HCl to 1-butyne would yield: CH_3CH_2CH_2CHCl_2 CH_3CH_2CCI_2CH_3 CH_3CH_2CHCICH_2Cl CH_3CH_2CH=CHCI CH_3CHCICHCICH_3 In the presence of excess hydrogen bromide, what is the major product of the addition of HBr to acetylene? 1, 3-dibromoethane 1-bromoethane 1, 1-dibromoethane 1, 2-dibromoethane 2-bromoethane Which of the following compounds is the major product when 1-hexyne is treated with excess HBr? 1, 1-dibromohexane 1, 1-dibromohexene 1, 2-dibromohexene 1, 2-dibromohexane 2, 2-dibromohexane
2. Which of the following compounds exhibit cis/trans Isomer CIS and transforms of the compounds that do exhibit Isomers s exhibit cis/trans isomerism? Explain why. Draw the a) Methylcyclobutane b) 3-ethyl-3-hexene c) 1-ethyl-3-methylcyclopentane d) 2,3-dimethylpentane e) 2,3-dichloro-2-hexene f) 2-butyne
10-2 Using acetylene as the starting material, show how you would synthesize the following compounds а) b) but-2-yne с) d)
_________________________________________________________________________________________________________________________________
d. Prepare octane from 1-pentyne, indicate each needed
reagents.
e. Synthesize cis-2-hexene from 1-pentyne and an alkyl
halide.
f. Synthesize trans-2-hexene from 1-pentyne and an alkyl
halide.
Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
VI. Starting from acetylene (CH C H) and using any needed reagents to synthesize the following molecule: Show every single step of the synthesis (10 pts)
please explain
Problem 5 (10 pts) Starting from acetylene propose a synthesis of both cis-3-heptene and trans-3-heptene.
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
Propose synthetic pathways for the laboratory preparation of the
following compounds from the specified substrates. Show all steps
complete with reagents and structures of products. Use any required
aliphatic and inorganic reagents.
i) propanal from 3-hexene j) 2-pentanone from butanoic acid k) 3-ethyl-3-pentanol from ethyl propanoate 1) 7-(N,N-dimethylamino)-2-heptanol from 1-methylcyclohexene
Most questions answered within 3 hours.
-
MATLAB
write a MATLAB function (1) output a third-order polynomial
function with the coefficients as the...
asked 3 minutes ago -
A z-score
communicates a raw score’s "relative standing"
under the normal curve in relation to:
asked 12 minutes ago -
An object is vibrating on a spring with the following equation
of motion:
?=(30 ??)cos((2?)/(160)?)
a)...
asked 11 minutes ago -
Vulcan Flyovers offers scenic overflights of Mount St. Helens,
the volcano in Washington State that explosively...
asked 13 minutes ago -
If organizations do not adapt fast enough and move incrementally
from the twentieth-century model to the...
asked 14 minutes ago -
A helium balloon with 2.5L of gas has a gauge pressure of 10,000
Pa. The balloon...
asked 18 minutes ago -
What is responsible for Jupiter's enormous magnetic field?
asked 34 minutes ago -
At the end of the year, a company offered to buy 5,000 units of
a product...
asked 35 minutes ago -
Implement C++ program for each of the following.
Let D = [-48, -14, -8, 0, 1,...
asked 55 minutes ago -
Consider a labor market in which LD = 400 – 4W and LS = 250 +...
asked 1 hour ago -
Let’s say you are teaching a typically-developing young child
how to eat with a spoon. Describe...
asked 53 minutes ago -
Ask Your Teacher A toy gun uses a spring to project a 5.6-g soft
rubber sphere...
asked 1 hour ago